Canonical Allele Identifier: CA1356009022
Gene: GLB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.33068822T= , CM000665.2:g.33068822T= GRCh38
NC_000003.11:g.33110314T= , CM000665.1:g.33110314T= GRCh37
NC_000003.10:g.33085318T= NCBI36
NG_009005.1:g.33381A=

Transcript Alleles

HGVS Amino-acid change
ENST00000307363.10:c.394A= MANE Select ENSP00000306920.4:p.Met132=
ENST00000307363.9:c.394A= ENSP00000306920.4:p.Met132=
ENST00000307377.12:c.246-3265A= ENSP00000305920.8:n.246-3265A=
ENST00000399402.7:c.304A= ENSP00000382333.2:p.Met102=
ENST00000415454.1:c.76-10553A= ENSP00000411813.1:n.76-10553A=
ENST00000438227.1:c.76-3265A= ENSP00000401250.1:n.76-3265A=
ENST00000440656.1:c.1A= ENSP00000411769.1:p.Met1=
ENST00000446732.5:c.156-3265A= ENSP00000407365.1:n.156-3265A=
ENST00000450835.1:c.304A= ENSP00000403264.1:p.Met102=
ENST00000464355.1:n.352A=
ENST00000482097.5:n.109-15273A=
ENST00000485698.5:n.137-15273A=
ENST00000498537.5:n.133-15273A=
NM_000404.2:c.394A= NP_000395.2:p.Met132=
NM_000404.3:c.394A= NP_000395.2:p.Met132=
NM_001079811.1:c.304A= NP_001073279.1:p.Met102=
NM_001079811.2:c.304A= NP_001073279.1:p.Met102=
NM_001135602.1:c.246-3265A= NP_001129074.1:n.246-3265A=
NM_001135602.2:c.246-3265A= NP_001129074.1:n.246-3265A=
NM_001317040.1:c.538A= NP_001303969.1:p.Met180=
NM_000404.4:c.394A= MANE Select NP_000395.3:p.Met132=
NM_001079811.3:c.304A= NP_001073279.2:p.Met102=
NM_001135602.3:c.246-3265A= NP_001129074.2:n.246-3265A=
NM_001317040.2:c.538A= NP_001303969.2:p.Met180=
NM_001393580.1:c.394A= NP_001380509.1:p.Met132=